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M Fanin

Showing results (11-20 of 68) with videos related to

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Human Mutation|June 30, 2000
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern ItalyM Fanin, E P Hoffman, C Angelini, et al.
Neuromuscular Disorders : NMD|July 19, 2003
LGMD2E patients risk developing dilated cardiomyopathyM Fanin, P Melacini, C Boito, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChRS Martignago, M Fanin, E Albertini, et al.
Journal of Medical Genetics|May 15, 2003
Novel sarcoglycan gene mutations in a large cohort of Italian patientsC Boito, M Fanin, G Siciliano, et al.
Journal of Clinical Pathology|January 29, 2005
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanismG Cenacchi, M Fanin, L B De Giorgi, et al.
Clinical Genetics|March 4, 2008
Cardioembolic stroke in Danon diseaseM Spinazzi, M Fanin, P Melacini, et al.
Cell Death and Differentiation|May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)A C Nascimbeni, M Fanin, E Masiero, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patientsM Fanin, G A Danieli, L Vitiello, et al.
Neurology|March 14, 2001
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathyM Fanin, E Pegoraro, C Matsuda-Asada, et al.
Neurology|November 9, 2000
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophyE Pegoraro, M Fanin, C P Trevisan, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Human Mutation|June 30, 2000
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern ItalyM Fanin, E P Hoffman, C Angelini, et al.
Neuromuscular Disorders : NMD|July 19, 2003
LGMD2E patients risk developing dilated cardiomyopathyM Fanin, P Melacini, C Boito, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChRS Martignago, M Fanin, E Albertini, et al.
Journal of Medical Genetics|May 15, 2003
Novel sarcoglycan gene mutations in a large cohort of Italian patientsC Boito, M Fanin, G Siciliano, et al.
Journal of Clinical Pathology|January 29, 2005
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanismG Cenacchi, M Fanin, L B De Giorgi, et al.
Clinical Genetics|March 4, 2008
Cardioembolic stroke in Danon diseaseM Spinazzi, M Fanin, P Melacini, et al.
Cell Death and Differentiation|May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)A C Nascimbeni, M Fanin, E Masiero, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patientsM Fanin, G A Danieli, L Vitiello, et al.
Neurology|March 14, 2001
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathyM Fanin, E Pegoraro, C Matsuda-Asada, et al.
Neurology|November 9, 2000
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophyE Pegoraro, M Fanin, C P Trevisan, et al.
Pageof 7